Canonical Allele Identifier: PA2827966781
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly1091Asp
CA008298
NM_001354898.2:c.3272G>A